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FDA 510(k)

P.O. VOX

K-Number: K860993 · 1986-04-25

Decision Date1986-04-25
Product CodeESE
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

P.O. VOX is the device name listed in this FDA 510(k) record. The listed applicant is Bloomfield Research and Development, Inc.. It received FDA 510(k) clearance on 1986-04-25 under 510(k) number K860993. The device is classified under product code ESE. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the P.O. VOX?

P.O. VOX is a medical device that received FDA 510(k) clearance on 1986-04-25. The listed applicant is Bloomfield Research and Development, Inc.. The 510(k) number is K860993.

When did P.O. VOX receive FDA 510(k) clearance?

P.O. VOX received FDA 510(k) clearance on 1986-04-25, under 510(k) number K860993.

Who is the listed applicant for P.O. VOX?

The FDA 510(k) record lists Bloomfield Research and Development, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for P.O. VOX?

The FDA product code for P.O. VOX is ESE.

Other records listing Bloomfield Research and Development, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Related Devices (Code: ESE)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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